Back to List
Share:
SHARE
Details:
Job Type:
Direct Hire
Remote Status:
On-Site
Apply Later:
Send this job to your inbox!
Our structural heart start-up client is growing their team and seeking a Clinical Science Specialist or Manager to support their expanding clinical and scientific programs. This individual will play a key role in driving the company’s scientific communications, data analysis, and evidence generation efforts across clinical, regulatory, and R&D functions.
Your role with the company:
Medical & Technical Writing
-
Develop a comprehensive understanding of the science behind the company’s products, competitive landscape, and disease areas.
-
Research, analyze, and write clinical and scientific documentation to support clinical, regulatory, and R&D functions.
-
Support R&D in planning and executing pre-clinical studies.
-
Develop and maintain scientific affairs procedures and best practices.
-
Summarize key takeaways from scientific meetings and conferences for internal teams.
Scientific Meeting & Publication Support
-
Maintain a global scientific meeting calendar, including key abstract submission deadlines (at least one year in advance).
-
Prepare abstracts and scientific presentations in collaboration with physician partners.
-
Identify and recommend relevant scientific meetings for data presentation and collaboration opportunities.
Desired Profile:
-
Master’s degree in Science or related field required; PhD preferred.
-
0–3 years of relevant scientific or medical writing experience.
-
Experience writing, editing, and submitting manuscripts for peer-reviewed publication.
-
Excellent scientific writing, communication, and presentation skills.
-
Strong organizational abilities and the capacity to manage multiple priorities in a fast-paced environment.
-
Collaborative, detail-oriented, and able to work independently.
-
Knowledge of cardiovascular anatomy, structural heart disease, and endovascular devices preferred.
-
Proficiency in Microsoft Office Suite.
-
Ability to travel up to 25%.
Apply to this Job
First Name *
Last Name *
Email Address *
Phone Number
Yes
No
Toggle Filters
Job Type
Remote Status
Create a Job Alert
Get notified about new listings!
Submit a Resume
Can't find the job you want?
Submit a general applicationJoin My Inner Circle
Featured
Minneapolis, MN
Direct Hire
Would you like to stay informed about new opportunities in the medical device manufacturing space? Join The Inner Circle Talent Database and gain exclusive access to roles and industry insights.
Your membership will remain completely confidential. No resumes or personal information will ever be shared without your explicit approval.
Why Join the Inner Circle?
Be the first to learn about exciting new roles.
Stay in the loop with industry trends and movements.
Gain access to exclusive opportunities with top-tier
Design Assurance Manager
10/21/2025
Minneapolis, MN
Direct HireOn-Site
Our mid-sized medical device client is adding a Design Assurance (DA) Manager to the team. The DA Manager will be responsible for providing quality engineering support for all phases of product development, driving post-market assessment activities, and supporting consistent design through production release and commercialization.
Your role with the company:
Responsible for ensuring staffing and successful execution for all projects assigned to the DA team. Serve as a working team member in the execution of product development process
Clinical Science Specialist/Manager
10/21/2025
Maple Grove, MN
Direct HireOn-Site Our structural heart start-up client is growing their team and seeking a Clinical Science Specialist or Manager to support their expanding clinical and scientific programs. This individual will play a key role in driving the company’s scientific communications, data analysis, and evidence generation efforts across clinical, regulatory, and R&D functions.
Your role with the company:
Medical & Technical Writing
Develop a comprehensive understanding of the science behind the company’s products, competitive landscape, and disease areas
Sr. Director of Clinical
10/16/2025
Minneapolis, MN
Direct Hire
Our mid-sized medical device client is adding a Senior Director of Clinical to the team. The Clinical Director is responsible for setting the clinical vision, leading clinical operations, and integrating clinical priorities into the company’s broader business strategy. This role demands a dynamic leader who can steer clinical innovation, navigate regulatory landscapes, and champion patient-centric outcomes while collaborating with the cross-functional teams to propel the company’s growth.
Your role with the company:
Clinical Vision &
Sr. Director of Regulatory Affairs
10/16/2025
Minneapolis, MN
Direct HireOn-Site Our science-driven medical device client is redefining expectations and advancing the field through cutting-edge solutions and therefore hiring a Sr. Director of Regulatory Affairs. The Sr. RA Director reports to the SVP of Clinical and Regulatory Affairs and will support the strategic direction, as well as lead the day-to-day execution of global regulatory activities. This role will be responsible for preparing high-quality regulatory submissions, supporting interactions with the FDA and other international regulatory bodies, and
Sr. Clinical Evidence Project Manager
10/16/2025
Minneapolis, MN
Direct HireHybrid Our mid-sized medical device client is adding a Senior Clinical Evidence Project Manager. The Project Manager will be responsible for the strategic management and oversight of all aspects of the Clinical Trial Team activities for assigned projects in accordance with the relevant standards as well as companies standard operating procedures. The Senior Clinical Evidence Project Manager, in collaboration with Clinical Program Managers and senior leadership, is accountable for achieving successful delivery of Clinical Team activities at the project level
Principal R&D Engineer
10/16/2025
Eden Prairie, MN
Direct HireOn-Site Our mid-size cardiovascular client is adding a Principal R&D/Product Development Engineer to the team. The Engineer will lead product development activities from concept to commercialization.
Your role with the company:
Lead conceptualization, design, and development of new devices or elements of new devices with the intent of commercialization per Quality System Requirements
Acts as leader and/or primary technical contributor for cross-functional development team(s) that manage projects from concept through commercialization.
Accurately and efficiently translates user
Production Supervisor (3rd shift)
10/16/2025
St. Paul, MN
Direct Hire Our mid-sized medical device client is recruiting for a Production Supervisor. The Production Supervisor will play a pivotal role in overseeing daily operations within manufacturing processes and ensuring adherence to policies and procedures. Your responsibilities will include developing people and processes to optimize safety, quality, productivity, and timely delivery. This role requires a blend of forward-thinking and hands-on leadership to drive operational excellence.
Your role with the company:
Lead assigned operations team in delivering results across the
Director of Business Development (mid-Atlantic)
10/16/2025
Westborough, MA
Direct HireFull Remote Our mid-sized client is adding a passionate and high-energy Director of Business Development to expand their national footprint. If you're a proven closer with a strategic mindset, experience in Urology, and a strong grasp of partnership contracts — we want to talk to you.
Our client provides state-of-the-art mobile healthcare services focused on advanced urology technologies — including shockwave lithotripsy (ESWL), laser lithotripsy (URS), and MR fusion biopsy. Their model is innovative, cost-effective, and deeply
(Sr) Clinical Research Associate
10/3/2025
Plymouth, MN
Direct HireHybrid Our start-up, clinical-stage medical device client, is adding a (Sr) Clinical Research Associate to the team. The CRA will support operational activities related to the organization's sponsored clinical research programs. Primary responsibilities will be the start-up and management of assigned clinical sites and task and projects related to the preparation and administration of US and OUS clinical trials, including (but not limited to) the development of study materials, site training materials, clinical quality system documents, device
Sr/Principal Regulatory Affairs Specialist
10/1/2025
Minneapolis, MN
Direct HireOn-Site
Our science-driven client is redefining expectations and advancing the field through cutting-edge solutions. The RA team is adding a Sr/Principal Regulatory Affairs Specialist to the team. The RA Specialist will report to the Director of RA and will lead and execute regulatory submission and approval activities for the company’s medical device products, with a primary focus on U.S. FDA submissions. This role will also provide support for international regulatory submissions outside North America. The Specialist will coordinate
Clinical Research Coordinator
9/29/2025
Maple Grove, MN
Direct HireOn-Site Our small start-up client is adding a Clinical Research Coordinator to the team. The CRC provides experienced administrative and logistical support to the Clinical Operations team. This role manages a broad range of trial coordination activities—from image and data tracking to documentation, payments, device logistics, and meeting support. The position flexes across responsibilities based on team workload, ensuring studies run smoothly and are audit-ready. The Clinical Coordinator is a key, stable member of the Clinical Operations group
Design Assurance Manager
9/29/2025
Minneapolis, MN
Direct Hire Our start-up medical device client is adding a Design Assurance Manager to the team. The DA Manager works cross-functionally and is responsible for providing Design Assurance representation on teams, facilitating design verification and validation for transfer to manufacturing, and implementing process/product improvements. The manager also supports quality management system process development and execution for applicable processes. The role has shared responsibility for product safety and quality in all stages of product and process development, and ensuring compliance with
Manufacturing Program Manager
9/29/2025
St Paul, MN
Direct HireOn-Site Our mid-sized medical device client is building a Program Management department. The Manufacturing Program Manager will oversee New Product Introductions, Capacity initiatives, and Transfer Programs. This role will work closely with plant leadership, quality, and the R&D group to create and establish a framework for oversight and management of NPI, Capacity Initiatives, and Transfer programs at manufacturing sites. This role works with internal and external customers, and technical resources are available to ensure effective execution of programs
Sr. R&D Engineer
9/29/2025
Minneapolis, MN
Direct HireOn-Site Our mid-size cardiovascular client is adding a Senior R&D/Product Development Engineer to the team. The Engineer will lead product development activities from concept to commercialization.
Your role with the company:
Lead conceptualization, design and development of new devices or elements of new devices with the intent of commercialization per Quality System Requirements
Acts as leader and/or primary technical contributor for cross-functional development team(s) that manage projects from concept through commercialization.
Accurately and efficiently translates user
Clinical Trial Assistant
8/5/2025
Plymouth, MN
Direct HireOn-Site Our clinical-stage medical device company is adding a Clinical Trial Assistant to the team. This position represents an exciting opportunity to make an impact in early stages of clinical development for an innovative technology. As a member of the field team, the Clinical Trial Assistant is a professional who provides administrative support to clinical trials. Their primary role is to assist clinical research professionals, such as clinical research coordinators, study managers, and investigators, with the daily tasks involved in
Sr. Clinical Research Associate
3/14/2025
St. Paul, MN
Direct HireHybrid Our small start-up client is adding (Sr.) Clinical Research Associates (CRA) to the team. The CRA works as part of the clinical team to ensure the completion of company-sponsored clinical studies. As an internal and externally facing position, this position interacts directly with the internal study team, clinical vendors, clinical Investigators, and other study staff at a clinical research site. The CRA will be the primary contact for the study sites regarding the proper execution of the clinical
Sr/Principal Product Development Engineer
3/14/2025
St. Paul, MN
Direct Hire Our mid-sized medical device client is looking for a seasoned engineer. The Product Development Engineer III with a mechanical focus, is responsible for development and implementation of new products, developed jointly with Process Development and Manufacturing Engineering, into full production, as well as supporting of continuation engineering on existing product lines. The role will be about 70% Project Management with about 30% technical.
Your role with the company:
Product Concept:
*Basic understanding of customer/user and patient needs.
*Proposes concepts
Loading Jobs...
